EP0705636A1 - Verbessertes Druckwechseladsorptionsverfahren - Google Patents

Verbessertes Druckwechseladsorptionsverfahren Download PDF

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EP0705636A1
EP0705636A1 EP95115794A EP95115794A EP0705636A1 EP 0705636 A1 EP0705636 A1 EP 0705636A1 EP 95115794 A EP95115794 A EP 95115794A EP 95115794 A EP95115794 A EP 95115794A EP 0705636 A1 EP0705636 A1 EP 0705636A1
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Prior art keywords
pressure
unit
gas
bed unit
adsorption
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French (fr)
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EP0705636B1 (de
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Mohamed Safdar Allie Baksh
Vincent John Kibler
Herbert Raymond Schaub
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Praxair Technology Inc
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Praxair Technology Inc
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    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/02—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by adsorption, e.g. preparative gas chromatography
    • B01D53/04—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by adsorption, e.g. preparative gas chromatography with stationary adsorbents
    • B01D53/047—Pressure swing adsorption
    • B01D53/0476—Vacuum pressure swing adsorption
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/02—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by adsorption, e.g. preparative gas chromatography
    • B01D53/04—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by adsorption, e.g. preparative gas chromatography with stationary adsorbents
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D2256/00—Main component in the product gas stream after treatment
    • B01D2256/12—Oxygen
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D2257/00—Components to be removed
    • B01D2257/10—Single element gases other than halogens
    • B01D2257/102—Nitrogen
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D2259/00—Type of treatment
    • B01D2259/40—Further details for adsorption processes and devices
    • B01D2259/40011—Methods relating to the process cycle in pressure or temperature swing adsorption
    • B01D2259/40028—Depressurization
    • B01D2259/40032—Depressurization with three sub-steps
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D2259/00—Type of treatment
    • B01D2259/40—Further details for adsorption processes and devices
    • B01D2259/40011—Methods relating to the process cycle in pressure or temperature swing adsorption
    • B01D2259/40043—Purging
    • B01D2259/4005—Nature of purge gas
    • B01D2259/40052—Recycled product or process gas
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D2259/00—Type of treatment
    • B01D2259/40—Further details for adsorption processes and devices
    • B01D2259/40011—Methods relating to the process cycle in pressure or temperature swing adsorption
    • B01D2259/40058—Number of sequence steps, including sub-steps, per cycle
    • B01D2259/40066—Six
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D2259/00—Type of treatment
    • B01D2259/40—Further details for adsorption processes and devices
    • B01D2259/40011—Methods relating to the process cycle in pressure or temperature swing adsorption
    • B01D2259/40077—Direction of flow
    • B01D2259/40081—Counter-current
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D2259/00—Type of treatment
    • B01D2259/40—Further details for adsorption processes and devices
    • B01D2259/401—Further details for adsorption processes and devices using a single bed
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D2259/00—Type of treatment
    • B01D2259/40—Further details for adsorption processes and devices
    • B01D2259/402—Further details for adsorption processes and devices using two beds
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/02—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by adsorption, e.g. preparative gas chromatography
    • B01D53/04—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by adsorption, e.g. preparative gas chromatography with stationary adsorbents
    • B01D53/047—Pressure swing adsorption
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/02—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by adsorption, e.g. preparative gas chromatography
    • B01D53/04—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by adsorption, e.g. preparative gas chromatography with stationary adsorbents
    • B01D53/047—Pressure swing adsorption
    • B01D53/0473—Rapid pressure swing adsorption
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/02—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by adsorption, e.g. preparative gas chromatography
    • B01D53/04—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by adsorption, e.g. preparative gas chromatography with stationary adsorbents
    • B01D53/047—Pressure swing adsorption
    • B01D53/053—Pressure swing adsorption with storage or buffer vessel

Definitions

  • the present invention relates to the separation of a first gas, such as oxygen gas, from a mixed gas such as air containing oxygen and other selectably-adsorbable gaseous components.
  • the object is to provide a more efficient pressure swing adsorption (PSA) process for the production of a concentrated gas, such as oxygen, from a gas mixture, such as air, which process utilizes the adsorbent in a more efficient manner (lower bed size factor), and requires less energy than other processes using prior art technology to produce high purity gas from gas mixtures.
  • PSA pressure swing adsorption
  • the PSA process is based upon the differential adsorption of selectively adsorbable gases and non-preferentially adsorbable gases, from mixtures thereof, on conventional adsorption bed materials such as zeolites.
  • the adsorption bed unit, or the first such bed unit of a two or three bed unit system each of which may contain a lower bed stratum for removing water and carbon dioxide and an upper or downstream bed stratum for adsorbing the selectively adsorbable gas from supply of a gas mixture passed therethrough, is pressurized to a high pressure value to cause the selective removal of water and carbon dioxide and the selective adsorption of the one gas, while the pressurized non-selectively adsorbable gas is unaffected and passes through to a reception unit, which may be the second bed unit of the system.
  • the second bed unit becomes pressurized by the non-adsorbed gas, preparatory to coming on stream in the next cycle.
  • the next bed unit i.e. a third bed unit or the first bed unit of a two bed system
  • the next bed unit is being cleaned by back-flow or countercurrent evacuation by passing a supply of medium pressure waste gas or void gas purged from-an equalization tank or from the bed unit being depressurized after producing the non-adsorbed, concentrated gas. This cleans the bed unit for subsequent repressurization and concentrated gas production.
  • the second bed unit is brought into sequential use, the first bed unit is evacuated and the second bed unit is repressurized.
  • the original PSA process was developed by Skarstrom, U.S. Patent 2,944,627, and consists of a cycle including four basic steps: (1) Adsorption, (2) Depressurization, (3) Purge, and (4) Repressurization.
  • Skarstrom cycle Several variations of the Skarstrom cycle have evolved.
  • One such system is described in Wagner U.S. Patent 3,430,418, wherein at least four beds are required to produce product continuously. The extra cost and complexity of providing four beds rather than a lesser number generally makes the Wagner system economically unfeasible.
  • Patent 5,223,004 described a PSA process utilizing the following steps: (1) a countercurrent product pressurization starting from the low pressure level of the cycle to an intermediate pressure level, (2) a cocurrent feed pressurization from the intermediate pressure level up to the adsorption pressure without bleeding off, (3) a production step wherein air is admitted and oxygen is bled off cocurrently, (4) a step where oxygen is bled off by partial depressurization cocurrently, wherein the admission of air is discontinued, and (5) a desorption step by depressurization countercurrently down to the low pressure level of the cycle.
  • U.S. Patent 4,194,891, 4,194,892 and 5,122,164 describe PSA cycles using short cycle times, wherein smaller particle size adsorbents are used to reduce diffusive resistance;
  • Doshi et al U.S. Patent 4,340,398, discloses a PSA process utilizing three or more beds, wherein void gas is transferred to a tank prior to bed regeneration, and later used for repressurization.
  • a process modification to a two-bed PSA process incorporating tank equalization is disclosed in U.S. Patents 3,788,036 and 3,142,547, where the conserved gas is used as the purge gas for another bed.
  • U.S. Patent 4,781,735 discloses a PSA process using three adsorbent beds to produce oxygen, with enhanced oxygen recovery achieved by connecting the feed end of one bed to the feed end of another bed (bottom-bottom equalization), and for all or part of the equalization time, top-top bed equalization is carried out simultaneously with the bottom-bottom equalization.
  • U.S. Patent 5,328,503, Kumar et al describes a PSA process that uses an initial depressurization step to provide a purge gas, followed by an optional bed-bed pressured equalization step.
  • at least two adsorbent beds are employed, and a combination of product and feed gas are used for repressurization of the adsorbent beds.
  • the present invention relates to an improved PSA process for separating a first gas, such as oxygen gas, from gas mixtures containing said first gas and one or more other gases including gases which are more preferentially adsorbable. It involves novel steps of simultaneous equalization and evacuation followed by simultaneous feed and product gas repressurization of PSA beds. This results in an overall faster and more efficient cycle with 100% utilization of a vacuum or pressure reducing blower, and a reduction in power use of about 15%.
  • a first gas such as oxygen gas
  • the heart of the invention involves overlapping of various steps of the PSA cycle to reduce total cycle time and thus improve productivity.
  • the other important parameters include choice of operating conditions (high pressure, low pressure, pressure at the end of equalization falling step, and the amount of high purity product used in the product pressurization step), the times allocated for each step, the order in which each step of the cycle is executed, and the use of equalization falling gas to provide the gas required for refluxing and equalization rising.
  • the unique step in the cycle is the step of simultaneously evacuating the bed undergoing the equalization rising step while the other bed is undergoing the equalization falling step.
  • the time allocated for this step must be chosen, so that at the end of this step, the former bed has been purged and also partially pressurized.
  • the next step in the cycle is simultaneous product and feed pressurization at opposite ends of said bed, followed by feed pressurization to the desired adsorption pressure.
  • Other key features of the invention are as follows: (a) the product gas required in the step of simultaneous feed and product pressurization usually comes from the product tank, or from another bed in the production step; and (b) the cocurrent depressurization or pressure equalization falling gas either goes to the downstream end of another bed or to a second storage tank. In the latter case, no bed-bed communication is required, which adds further flexibility in controlling the PSA process.
  • the novel process of the present invention incorporates a novel sequence of operating steps in the PSA cycle, wherein the unload times for rotary machines (e.g. compressors and vacuum pumps) are minimized, product recovery is enhanced, the bed size factor (BSF) is comparable or lower than with prior art PSA cycles, and the power consumption is 5-20% lower than prior known PSA cycles.
  • the operating steps in the present PSA cycle are as follows:
  • Fig. 1 The above steps are shown schematically in Fig. 1 for a two-bed PSA process.
  • BSF bed size factor
  • the equalization falling gas provides all of the gas needed by another bed that is undergoing equalization rising and evacuation simultaneously.
  • this step overlaps the equalization step with the purge step, thereby modifying the conventional purge step and equalization step used in prior art PSA cycles.
  • all of the reflux gas necessary to push the nitrogen wavefront out of the bed is provided by the other bed going through the equalization falling step.
  • lower purity gas is used for the combined purging and equalization rising steps.
  • the next step in the cycle uses high purity product gas, usually from the product tank, to pressurize the column at the product end, while feed gas is simultaneously fed at the other end of the bed.
  • the invention consists of the overlapping of various steps in the PSA cycle to reduce total cycle time and thus improve productivity, the choice of operating conditions (high pressure, low pressure, pressure at the end of the equalization falling step, and the amount of high purity product used in step 1 of Fig. 1), the times allocated for each step, the order in which each step of the cycle is executed, and the use of equalization falling gas to provide the gas required for refluxing and equalization rising.
  • the unique step in the cycle is step III (see Fig. 1), wherein the bed undergoing the equalization falling step is opened to another bed which is simultaneously being pressurized and evacuated. The time allocated for this step must be chosen so that at the end of this step, the second bed has been purged and partially pressurized.
  • the next step in the cycle is simultaneous product and feed pressurization at opposite ends of the second bed, followed by feed pressurization to the adsorption pressure, step IIA, Figure 3.
  • FIG. 1 is a schematic diagram of a two-bed PSA process consisting of the two adsorption beds A and B of Fig. 1, feed compressor(s) or blower(s) 11, vacuum pump(s) 13, product storage tank 18 and interconnected lines and valves.
  • Fig. 3 shows the evolution of pressure during the execution of the various steps of the cycle, with the cycle starting after step 6 in Fig. 1. Referring to Figs. 1, 2 and 3, the PSA process is disclosed for a complete cycle.
  • the PSA process of Fig. 2 consists of two beds (A & B) filled with adsorbents, each having an inlet valve 33 or 35, and an outlet valve 34 or 36.
  • the feed inlet valves 33 and 35 are connected to an air supply conduit 10 through a blower machine or compressor 11; whereas the exhaust outlet valves 34 and 36 are connected to a vacuum exhaust conduit 12 incorporating a vacuum pump 13.
  • the bed outlet conduits 14 and 15 communicate with valves 5 and 6 to a production conduit 16 through a control valve 17 that connects to a product storage tank 18.
  • Valves 10A and 12A allow the two beds to communicate if a purge gas step is included in the cycle.
  • valve 12A when opened, allows a portion of the product gas from bed A to supply a purge stream to bed B.
  • valve 10A when opened, allows a portion of the product gas from bed B to supply the purge gas to bed A.
  • the outlet conduits 14 and 15 are connected to each other by valves 2 and 4. All the valves in the diagram are operated electronically via a computer system and program logic.
  • Conduit 19 is connected to the product storage tank, and supplies product gas, via valves 8 and 9, for product pressurization of beds B and A, respectively.
  • Figs. 1 and 2 the novel VPSA O2 process for a two-bed system is now described to illustrate the opening and closing of the valves for each step of the cycle. All valves are closed except those indicated in each step.
  • the cycle time is about 60 seconds and the pressure ranges between a low of 0.35 atm. and a high of 2.0 atm.
  • Step I Feed (air) through line 10, and product (oxygen), from tank 18, are introduced simultaneously at opposite ends of the bed.
  • valves 33 and 9 are opened to allow feed and product gas to enter the bed, respectively.
  • valve 36 is opened and the other bed B is undergoing evacuation.
  • Step II In the feed pressurization and gross product make step, valves 33 and 5 are open and bed A undergoes further feed pressurization. Control valve 17 program logic dictates when this valve will be opened to allow product gas to enter the product tank 18 from bed A. For instance, if constant pressure is required during the make product steps, then control valve 17 only opens when bed A reaches a predetermined pressure level to allow product to enter the product tank 18. During the feed pressurization and make product step (step 2) for bed A, bed B is undergoing evacuation via valve 36.
  • Step III Cocurrent depressurization.
  • valve 33 is closed, and valve 4 is opened to recover the void gas from bed A and direct it to bed B to partially pressurize bed B (equalization rising for bed B), and as reflux gas to push the nitrogen wavefront in bed B towards the feed end thereof.
  • valve 36 is still opened, thus bed B undergoes equalization rising and evacuation simultaneously.
  • Another version of this invention collects the equalization falling void gas into a separate storage tank for supply to bed B. In this latter case, no bed-bed communication is necessary.
  • Step IV Valve 34 is now opened to evacuate bed A countercurrently, and valves 35 and 8 are opened so that bed B undergoes simultaneous feed and product pressurization from opposite ends.
  • Step V Valve 34 is still opened with bed A undergoing further evacuation, while valve 35 and 6 are opened so that bed B is pressurized with feed to the adsorption pressure.
  • Control valve 17 logic determines when product gas from bed B enters the product tank 18.
  • Step VI Valve 35 is closed, and bed B undergoes depressurization via valve 2 that connects bed A or a second storage tank, which in turn provides the increasing pressure purge to bed A. During this time, valve 34 is still in the opened position, allowing bed A to undergo equalization rising and evacuation simultaneously.
  • the countercurrent depressurization step IV can be preceded by opening to air until the pressure in the bed drops to 1.0 atm., then evacuation begins.
  • the two-bed process of Fig. 2 utilizing the steps of Fig. 1 can produce comparable oxygen purity and recovery with lower bed size and lower power consumption, as compared to the standard process depicted in Fig. 8. Also, in this process, the vacuum pump is used continuously by one or the other bed during each step of the cycle. Bed size reduction and power reduction achieved are in the range of about 5 to 20%
  • Figures 4 and 5 show an alternate system for operating a two-bed PSA process that utilizes a product storage vessel 18 and an equalization tank 20.
  • the execution of the various steps, including the opening and closing of the valves, is similar to the description given above for Fig. 2.
  • the use of two storage vessels allows for greater flexibility in the process.
  • the individual steps in the cycle shown in Fig. 5 do not have to occupy fixed periods of time.
  • physical variables such as pressure and composition can be used easily to determine the time allocated for each step, thereby adjusting the process for changes in temperature, pressure and variable product demand. Since no bed-bed gas transfer is required, then it is possible to run each bed independently, and regard the process as a collection of single bed units.
  • some synchronization of the overall cycle of each bed with the cycles of the other beds is necessary.
  • the apparatus of the present invention preferably makes use of cylindrical adsorbent beds with shallow dished heads on the top and bottom, and gas flow in the axial direction
  • bed configurations can be used.
  • radial beds may be used to achieve a reduction in pressure losses with a concomitant reduction in power consumption.
  • layered beds can be used with different adsorbents packed at various positions in the bed.
  • activated alumina can be placed at the feed end of the bed to remove water and carbon dioxide from the feed stream
  • Li-X zeolite can be placed on top of the activated alumina to perform the separation of air into an oxygen enriched product.
  • the two bed system and process of Figs. 4 and 5 provide improvements comparable to those provided by the system and process of Figs. 1, 2 and 3 but with a slight improvement in the product recovery rate.
  • Figs. 6 and 7 of the drawings illustrate the use of a single bed process utilizing a product tank 18 and an equalization tank 20.
  • the process of Fig. 6 shows a single compressor/blower 11 used to perform the pressurization and evacuation steps illustrated in Fig. 7. Referring to Figs. 6 and 7, the steps in the cycle are briefly described.
  • valves 9, 10 and 33 are opened and the other valves are closed.
  • Valve 17 is a differential pressure check valve that opens only when the pressure in the adsorbent vessel C becomes greater than the pressure in the product tank 18. After some time, valve 9 closes, and step 2 begins.
  • feed pressurization continues via valves 10 and 33, differential check valve 17 opens and product gas enters the product storage tank 18.
  • valve 33 is closed, and valve 36 is opened to unload the compressor 11. During this time, the bed undergoes cocurrent depressurization with valve 4 in the opened position to collect the void gas into the equalization tank 20.
  • step III the check valve 17 will be in the closed position during the cocurrent depressurization step (step III), since the pressure of the adsorbent bed C will fall below that of the product tank (18).
  • step III execution, valves 9, 10 and 33 are in the closed positions.
  • valves 12 and 34 are in the opened positions, while valves 4, 9, 10, 17, 33 and 36 are closed.
  • step IV gas in the adsorbent vessel C leaves via valve 34 and enters through the inlet of the compressor.
  • step V is just a continuation of step IV (evacuation step).
  • step VI is executed with valves 12 and 34 still in the open positions. During this step, valve 4 is opened, and the gas from the equalization tank 20 provides the reflux gas to desorb the adsorbed gas and to partially pressurize the bed C.
  • Fig. 8 illustrates a conventional PSA process using a prior art cycle with cycle time about 10 to 20% greater than that of the present invention.
  • the novel cycle has been described in relation to VPSA O2 processes, wherein particular embodiments of the invention have been shown, other embodiments are contemplated along with modification of the disclosed features, as being within the scope of the claims.
  • the novel cycle is not restricted to transatmospheric vacuum pressure swing adsorption (VPSA) cycles, and super atmospheric or subatmospheric pressure swing adsorption cycles may also be used.
  • VPSA transatmospheric vacuum pressure swing adsorption
  • super atmospheric or subatmospheric pressure swing adsorption cycles may also be used.
  • pressurized “high pressure”, “medium pressure”, “depressurization”, etc.
  • gas under a small vacuum pressure is “pressurized” or at a “high pressure” relative to gas under a higher vacuum or negative pressure.
  • the novel cycle can be used in other mixture separations, e.g., N2/CH4 separation from landfill gas, and other gas mixtures for example feeds containing hydrogen as the nonpreferentially adsorbed product component and various impurities as selectively adsorbable components.
  • feeds containing hydrogen include light hydrocarbons, CO, CO2, NH3, H2S, argon and water.
  • Hydrogen-rich feed gas containing at least one of these adsorbable components include: catalytic reformer off-gas, methanol synthesis loop purge, dissociated ammonia and demethanizer over-head gas, steam-reformed hydrocarbons, ammonia synthesis loop purge gas, electrolytic hydrogen and mercury cell hydrogen.
  • the invention is also useful for separating any or all of the aforementioned adsorbables from gas mixtures in which nitrogen or helium is the primary constituent.
  • the present invention provides a novel vacuum pressure swing adsorption process for producing a concentrated gas from gas mixtures, involving the novel steps of simultaneous equalization and evacuation of the adsorption bed in one step, followed by simultaneous product and feed repressurization of the adsorption bed in another step, resulting in an overall faster and more efficient process in which the vacuum blower is utilized full time and power consumption is reduced by about 15%.
  • the novel process of the present invention can be conducted at pressure levels which are superatmospheric, transatmospheric or subatmospheric, and applies to the separation of gases in general, using PSA process systems.

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Analytical Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Separation Of Gases By Adsorption (AREA)
  • Oxygen, Ozone, And Oxides In General (AREA)
  • Gas Separation By Absorption (AREA)
EP95115794A 1994-10-07 1995-10-06 Verbessertes Druckwechseladsorptionsverfahren Expired - Lifetime EP0705636B1 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US319692 1994-10-07
US08/319,692 US5518526A (en) 1994-10-07 1994-10-07 Pressure swing adsorption process

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EP0705636A1 true EP0705636A1 (de) 1996-04-10
EP0705636B1 EP0705636B1 (de) 1999-12-29

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US (1) US5518526A (de)
EP (1) EP0705636B1 (de)
JP (1) JP3325167B2 (de)
KR (1) KR100260001B1 (de)
CN (1) CN1080136C (de)
BR (1) BR9504315A (de)
CA (1) CA2160046C (de)
DE (1) DE69514190T2 (de)
ES (1) ES2139812T3 (de)
MX (1) MX9504250A (de)
TW (1) TW297780B (de)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0771583A1 (de) * 1995-11-06 1997-05-07 Praxair Technology, Inc. Druckwechseladsorptionsverfahren mit einzigem Bett zur Gewinnung von Sauerstoff aus Luft
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EP0771583A1 (de) * 1995-11-06 1997-05-07 Praxair Technology, Inc. Druckwechseladsorptionsverfahren mit einzigem Bett zur Gewinnung von Sauerstoff aus Luft
EP0853968A1 (de) * 1997-01-15 1998-07-22 Praxair Technology, Inc. Verfahren zur Herstellung von Stickstoff mittels eines sauerstoffselektiven Sorptionsmittels
EP0868936A1 (de) * 1997-04-02 1998-10-07 L'air Liquide, Societe Anonyme Pour L'etude Et L'exploitation Des Procedes Georges Claude Verfahren und Vorrichtung zur Trennung einer Gasmischung durch Adsorption
FR2761616A1 (fr) * 1997-04-02 1998-10-09 Air Liquide Procede et installation de separation d'un melange gazeux par adsorption
US5964924A (en) * 1997-04-02 1999-10-12 L'air Liquide, Societe Anonyme Pour L'etude Et L'exploitation Des Procedes Georges Claude Process and installation for the separation of a gas mixture by adsorption
EP0873776A2 (de) * 1997-04-23 1998-10-28 The Boc Group, Inc. Druckwechseladsorptionsverfahren und -vorrichtung
EP0873776A3 (de) * 1997-04-23 1998-11-18 The Boc Group, Inc. Druckwechseladsorptionsverfahren und -vorrichtung
KR100278323B1 (ko) * 1997-04-23 2001-01-15 페이스 살바토르 피 압력스윙흡착방법및장치
EP1203610B1 (de) * 2000-11-01 2005-12-21 Air Products And Chemicals, Inc. Einzelbett Druckwechseladsorptionsverfahren
WO2002049959A1 (fr) * 2000-12-19 2002-06-27 Sumitomo Seika Chemicals Co., Ltd. Procede de recuperation d'oxygene gazeux enrichi
US6663691B2 (en) 2000-12-19 2003-12-16 Sumitomo Seika Chemicals Co., Ltd. Method of recovering enriched gaseous oxygen
US9579598B2 (en) 2015-05-15 2017-02-28 Apache Corporation Pressure swing adsorption process for enhanced separation of lighter from heavier species

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EP0705636B1 (de) 1999-12-29
BR9504315A (pt) 1997-04-08
JPH08309139A (ja) 1996-11-26
JP3325167B2 (ja) 2002-09-17
CN1133199A (zh) 1996-10-16
CA2160046A1 (en) 1996-04-08
DE69514190T2 (de) 2000-08-17
US5518526A (en) 1996-05-21
ES2139812T3 (es) 2000-02-16
CA2160046C (en) 2000-12-26
CN1080136C (zh) 2002-03-06
TW297780B (de) 1997-02-11
KR100260001B1 (ko) 2000-06-15
KR960013429A (ko) 1996-05-22
DE69514190D1 (de) 2000-02-03

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